Asymmetric synthesis of amino sugars. Part 1: Stereoselective synthesis of(2S,3S,4R,5S)-2-amino-1,3,4,5,6-hexanepentol derivatives and their conversion to L-mannosamine derivatives

Citation
L. Ermolenko et al., Asymmetric synthesis of amino sugars. Part 1: Stereoselective synthesis of(2S,3S,4R,5S)-2-amino-1,3,4,5,6-hexanepentol derivatives and their conversion to L-mannosamine derivatives, TETRAHEDR L, 40(28), 1999, pp. 5187-5190
Citations number
33
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
40
Issue
28
Year of publication
1999
Pages
5187 - 5190
Database
ISI
SICI code
0040-4039(19990709)40:28<5187:ASOASP>2.0.ZU;2-P
Abstract
A novel approach for asymmetric synthesis of amino sugars is developed, sta rting from readily available chiral building blocks 1 and 2,3-O-isopropylid eneglyceraldehyde 2, via the Julia olefination and subsequent dihydroxylati on as key steps. (C) 1999 Published by Elsevier Science Ltd. All rights res erved.